Please choose an event type to view the corresponding MedsFacts report:

NAUSEA ( 60 FDA reports)
PAIN ( 45 FDA reports)
HEADACHE ( 39 FDA reports)
ASTHENIA ( 38 FDA reports)
BLOOD PRESSURE INCREASED ( 37 FDA reports)
FATIGUE ( 37 FDA reports)
PAIN IN EXTREMITY ( 35 FDA reports)
DYSPNOEA ( 34 FDA reports)
DIZZINESS ( 33 FDA reports)
ANXIETY ( 32 FDA reports)
DRUG INEFFECTIVE ( 32 FDA reports)
HYPOAESTHESIA ( 31 FDA reports)
WEIGHT DECREASED ( 30 FDA reports)
BACK PAIN ( 29 FDA reports)
DIARRHOEA ( 27 FDA reports)
HYPERTENSION ( 25 FDA reports)
OEDEMA PERIPHERAL ( 23 FDA reports)
VOMITING ( 23 FDA reports)
CEREBROVASCULAR ACCIDENT ( 22 FDA reports)
MYOCARDIAL INFARCTION ( 22 FDA reports)
URTICARIA ( 22 FDA reports)
EMOTIONAL DISTRESS ( 21 FDA reports)
PAIN IN JAW ( 21 FDA reports)
RASH ( 21 FDA reports)
DYSPHAGIA ( 20 FDA reports)
HYPONATRAEMIA ( 20 FDA reports)
INFLAMMATION ( 20 FDA reports)
BONE DISORDER ( 19 FDA reports)
BONE PAIN ( 19 FDA reports)
INSOMNIA ( 19 FDA reports)
MUSCLE SPASMS ( 19 FDA reports)
PRIMARY SEQUESTRUM ( 19 FDA reports)
CORONARY ARTERY DISEASE ( 18 FDA reports)
DEFORMITY ( 17 FDA reports)
FALL ( 17 FDA reports)
RENAL FAILURE ( 17 FDA reports)
ANAEMIA ( 16 FDA reports)
ANHEDONIA ( 16 FDA reports)
ARTHRALGIA ( 16 FDA reports)
CARDIAC FAILURE CONGESTIVE ( 16 FDA reports)
DYSGEUSIA ( 16 FDA reports)
PROCEDURAL PAIN ( 16 FDA reports)
SPINAL OSTEOARTHRITIS ( 16 FDA reports)
TOOTHACHE ( 16 FDA reports)
ACTINOMYCOSIS ( 15 FDA reports)
COUGH ( 15 FDA reports)
DEPRESSION ( 15 FDA reports)
DERMATITIS ( 15 FDA reports)
OSTEOMYELITIS ( 15 FDA reports)
PAPILLOMA ( 15 FDA reports)
PRURITUS ( 15 FDA reports)
RENAL FAILURE ACUTE ( 15 FDA reports)
VISION BLURRED ( 15 FDA reports)
ABSCESS JAW ( 14 FDA reports)
ASPIRATION ( 14 FDA reports)
DENTAL CARIES ( 14 FDA reports)
DIABETES MELLITUS ( 14 FDA reports)
DRUG INTERACTION ( 14 FDA reports)
FACE OEDEMA ( 14 FDA reports)
FEELING ABNORMAL ( 14 FDA reports)
FISTULA ( 14 FDA reports)
GAIT DISTURBANCE ( 14 FDA reports)
GINGIVAL SWELLING ( 14 FDA reports)
HYPERGLYCAEMIA ( 14 FDA reports)
HYPERPLASIA ( 14 FDA reports)
IMPAIRED HEALING ( 14 FDA reports)
MYOFASCIAL PAIN SYNDROME ( 14 FDA reports)
ORAL CAVITY FISTULA ( 14 FDA reports)
ORAL DISCOMFORT ( 14 FDA reports)
OSTEOARTHRITIS ( 14 FDA reports)
OSTEONECROSIS OF JAW ( 14 FDA reports)
TOOTH FRACTURE ( 14 FDA reports)
TOOTH INFECTION ( 14 FDA reports)
TOOTH LOSS ( 14 FDA reports)
URINARY TRACT INFECTION ( 14 FDA reports)
ATRIAL FIBRILLATION ( 13 FDA reports)
BLOOD GLUCOSE INCREASED ( 13 FDA reports)
CHEST PAIN ( 13 FDA reports)
CHILLS ( 13 FDA reports)
HYPERHIDROSIS ( 13 FDA reports)
PURULENT DISCHARGE ( 13 FDA reports)
TOOTH DEPOSIT ( 13 FDA reports)
TOOTH DISORDER ( 13 FDA reports)
ABDOMINAL PAIN ( 12 FDA reports)
DEHYDRATION ( 12 FDA reports)
INJURY ( 12 FDA reports)
INTERVERTEBRAL DISC PROTRUSION ( 12 FDA reports)
MYALGIA ( 12 FDA reports)
SYNCOPE ( 12 FDA reports)
BLOOD PRESSURE INADEQUATELY CONTROLLED ( 11 FDA reports)
CONSTIPATION ( 11 FDA reports)
DYSPEPSIA ( 11 FDA reports)
HYPERKALAEMIA ( 11 FDA reports)
PLEURAL EFFUSION ( 11 FDA reports)
TREMOR ( 11 FDA reports)
WEIGHT INCREASED ( 11 FDA reports)
BLOOD CHOLESTEROL INCREASED ( 10 FDA reports)
CERVICAL SPINAL STENOSIS ( 10 FDA reports)
CONDITION AGGRAVATED ( 10 FDA reports)
GASTROOESOPHAGEAL REFLUX DISEASE ( 10 FDA reports)
HYPOKALAEMIA ( 10 FDA reports)
INJECTION SITE BRUISING ( 10 FDA reports)
KYPHOSIS ( 10 FDA reports)
LACUNAR INFARCTION ( 10 FDA reports)
PALPITATIONS ( 10 FDA reports)
PYREXIA ( 10 FDA reports)
SKIN LESION ( 10 FDA reports)
ATELECTASIS ( 9 FDA reports)
CHOLECYSTITIS ( 9 FDA reports)
EPISTAXIS ( 9 FDA reports)
HYPERSENSITIVITY ( 9 FDA reports)
ARTHRITIS ( 8 FDA reports)
BRONCHITIS ( 8 FDA reports)
DIABETES MELLITUS INADEQUATE CONTROL ( 8 FDA reports)
DIVERTICULITIS ( 8 FDA reports)
DIVERTICULUM ( 8 FDA reports)
DRUG WITHDRAWAL SYNDROME ( 8 FDA reports)
DRY MOUTH ( 8 FDA reports)
FLATULENCE ( 8 FDA reports)
GASTRITIS ( 8 FDA reports)
GOUT ( 8 FDA reports)
HERPES ZOSTER ( 8 FDA reports)
HYPOGLYCAEMIA ( 8 FDA reports)
INJECTION SITE DISCOLOURATION ( 8 FDA reports)
INJECTION SITE ERYTHEMA ( 8 FDA reports)
JAW OPERATION ( 8 FDA reports)
MALAISE ( 8 FDA reports)
METASTASES TO BONE ( 8 FDA reports)
ORAL SURGERY ( 8 FDA reports)
PARAESTHESIA ( 8 FDA reports)
RESPIRATORY FAILURE ( 8 FDA reports)
SKIN DISORDER ( 8 FDA reports)
SKIN EXFOLIATION ( 8 FDA reports)
TOOTH EXTRACTION ( 8 FDA reports)
ANGIOEDEMA ( 7 FDA reports)
AORTIC CALCIFICATION ( 7 FDA reports)
BLOOD ALKALINE PHOSPHATASE INCREASED ( 7 FDA reports)
BURNS THIRD DEGREE ( 7 FDA reports)
COMPRESSION FRACTURE ( 7 FDA reports)
DENTAL OPERATION ( 7 FDA reports)
DISEASE PROGRESSION ( 7 FDA reports)
DIVERTICULUM INTESTINAL ( 7 FDA reports)
DRUG TOXICITY ( 7 FDA reports)
FISTULA REPAIR ( 7 FDA reports)
HYPERBARIC OXYGEN THERAPY ( 7 FDA reports)
INJECTION SITE ANAESTHESIA ( 7 FDA reports)
INJECTION SITE INDURATION ( 7 FDA reports)
INJECTION SITE IRRITATION ( 7 FDA reports)
INJECTION SITE NECROSIS ( 7 FDA reports)
INJECTION SITE PAIN ( 7 FDA reports)
INJECTION SITE SWELLING ( 7 FDA reports)
INTERNATIONAL NORMALISED RATIO INCREASED ( 7 FDA reports)
METASTASES TO SPINE ( 7 FDA reports)
NEOPLASM MALIGNANT ( 7 FDA reports)
NEOPLASM PROGRESSION ( 7 FDA reports)
NEPHROGENIC SYSTEMIC FIBROSIS ( 7 FDA reports)
OSTEONECROSIS ( 7 FDA reports)
PALLOR ( 7 FDA reports)
PATHOLOGICAL FRACTURE ( 7 FDA reports)
PLASTIC SURGERY TO THE FACE ( 7 FDA reports)
PNEUMONIA ( 7 FDA reports)
RENAL ARTERY STENOSIS ( 7 FDA reports)
SURGERY ( 7 FDA reports)
SWELLING FACE ( 7 FDA reports)
TACHYCARDIA ( 7 FDA reports)
ALOPECIA ( 6 FDA reports)
APPETITE DISORDER ( 6 FDA reports)
BLISTER ( 6 FDA reports)
BLOOD PRESSURE FLUCTUATION ( 6 FDA reports)
BRONCHOPNEUMONIA ( 6 FDA reports)
CARDIAC DISORDER ( 6 FDA reports)
CELLULITIS ( 6 FDA reports)
CENTRAL VENOUS CATHETERISATION ( 6 FDA reports)
CHEST WALL MASS ( 6 FDA reports)
CHRONIC OBSTRUCTIVE PULMONARY DISEASE ( 6 FDA reports)
COLITIS ISCHAEMIC ( 6 FDA reports)
DEBRIDEMENT ( 6 FDA reports)
DECREASED APPETITE ( 6 FDA reports)
DIAPHRAGMATIC HERNIA ( 6 FDA reports)
EAR PAIN ( 6 FDA reports)
GENERAL PHYSICAL HEALTH DETERIORATION ( 6 FDA reports)
GINGIVAL EROSION ( 6 FDA reports)
HAEMOGLOBIN DECREASED ( 6 FDA reports)
HEART RATE DECREASED ( 6 FDA reports)
HEART RATE IRREGULAR ( 6 FDA reports)
HYPERURICAEMIA ( 6 FDA reports)
HYPOXIA ( 6 FDA reports)
INTESTINAL ISCHAEMIA ( 6 FDA reports)
INTESTINAL RESECTION ( 6 FDA reports)
MALIGNANT PLEURAL EFFUSION ( 6 FDA reports)
MYELOMA RECURRENCE ( 6 FDA reports)
NERVOUSNESS ( 6 FDA reports)
PANCREATITIS ACUTE ( 6 FDA reports)
PNEUMONIA PRIMARY ATYPICAL ( 6 FDA reports)
PROTEINURIA ( 6 FDA reports)
PRURITUS GENERALISED ( 6 FDA reports)
SKIN PAPILLOMA ( 6 FDA reports)
SKIN ULCER ( 6 FDA reports)
SPINAL HAEMANGIOMA ( 6 FDA reports)
STREPTOCOCCAL INFECTION ( 6 FDA reports)
TRANSIENT ISCHAEMIC ATTACK ( 6 FDA reports)
VASCULAR PSEUDOANEURYSM ( 6 FDA reports)
WOUND DRAINAGE ( 6 FDA reports)
ABDOMINAL PAIN UPPER ( 5 FDA reports)
ACUTE CORONARY SYNDROME ( 5 FDA reports)
ALANINE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
ASPARTATE AMINOTRANSFERASE INCREASED ( 5 FDA reports)
BILE DUCT STONE ( 5 FDA reports)
CARDIAC FAILURE ( 5 FDA reports)
DECUBITUS ULCER ( 5 FDA reports)
ENDODONTIC PROCEDURE ( 5 FDA reports)
GINGIVAL INFECTION ( 5 FDA reports)
HAEMOPTYSIS ( 5 FDA reports)
HOT FLUSH ( 5 FDA reports)
LOW DENSITY LIPOPROTEIN INCREASED ( 5 FDA reports)
MUSCULAR WEAKNESS ( 5 FDA reports)
MYOCARDIAL ISCHAEMIA ( 5 FDA reports)
NECK PAIN ( 5 FDA reports)
NEPHROTIC SYNDROME ( 5 FDA reports)
OVERDOSE ( 5 FDA reports)
PALMAR-PLANTAR ERYTHRODYSAESTHESIA SYNDROME ( 5 FDA reports)
PHARMACEUTICAL PRODUCT COMPLAINT ( 5 FDA reports)
PLATELET COUNT DECREASED ( 5 FDA reports)
POLLAKIURIA ( 5 FDA reports)
RED BLOOD CELL COUNT DECREASED ( 5 FDA reports)
RENAL IMPAIRMENT ( 5 FDA reports)
RHABDOMYOLYSIS ( 5 FDA reports)
SKIN BURNING SENSATION ( 5 FDA reports)
SNEEZING ( 5 FDA reports)
STRESS ( 5 FDA reports)
VENTRICULAR EXTRASYSTOLES ( 5 FDA reports)
WHITE BLOOD CELL COUNT DECREASED ( 5 FDA reports)
ABDOMINAL PAIN LOWER ( 4 FDA reports)
ANGINA PECTORIS ( 4 FDA reports)
ANGINA UNSTABLE ( 4 FDA reports)
BASAL CELL CARCINOMA ( 4 FDA reports)
BONE MARROW DISORDER ( 4 FDA reports)
C-REACTIVE PROTEIN INCREASED ( 4 FDA reports)
CARDIOVASCULAR DISORDER ( 4 FDA reports)
CHEST DISCOMFORT ( 4 FDA reports)
COLONIC POLYP ( 4 FDA reports)
CONFUSIONAL STATE ( 4 FDA reports)
DYSKINESIA ( 4 FDA reports)
ENCEPHALOPATHY ( 4 FDA reports)
EXCORIATION ( 4 FDA reports)
EXFOLIATIVE RASH ( 4 FDA reports)
FEAR ( 4 FDA reports)
FLUSHING ( 4 FDA reports)
FREQUENT BOWEL MOVEMENTS ( 4 FDA reports)
GAMMA-GLUTAMYLTRANSFERASE INCREASED ( 4 FDA reports)
GASTRIC DISORDER ( 4 FDA reports)
GENERALISED OEDEMA ( 4 FDA reports)
HAEMATURIA ( 4 FDA reports)
HAEMORRHOIDS ( 4 FDA reports)
HALLUCINATION ( 4 FDA reports)
HYPOAESTHESIA ORAL ( 4 FDA reports)
HYPOTENSION ( 4 FDA reports)
LOSS OF CONSCIOUSNESS ( 4 FDA reports)
LUNG DISORDER ( 4 FDA reports)
MALIGNANT HYPERTENSION ( 4 FDA reports)
MELAENA ( 4 FDA reports)
MENTAL STATUS CHANGES ( 4 FDA reports)
MOBILITY DECREASED ( 4 FDA reports)
NEPHROPATHY ( 4 FDA reports)
NEURODERMATITIS ( 4 FDA reports)
PANCREATITIS ( 4 FDA reports)
PRIAPISM ( 4 FDA reports)
PRODUCT COUNTERFEIT ( 4 FDA reports)
PRODUCT QUALITY ISSUE ( 4 FDA reports)
PULSE ABSENT ( 4 FDA reports)
RASH GENERALISED ( 4 FDA reports)
RECTAL HAEMORRHAGE ( 4 FDA reports)
SKIN CANCER ( 4 FDA reports)
SKIN DISCOLOURATION ( 4 FDA reports)
SLEEP DISORDER ( 4 FDA reports)
SOMNOLENCE ( 4 FDA reports)
SUPRAVENTRICULAR EXTRASYSTOLES ( 4 FDA reports)
SWELLING ( 4 FDA reports)
VISUAL DISTURBANCE ( 4 FDA reports)
WHITE BLOOD CELL COUNT INCREASED ( 4 FDA reports)
ABDOMINAL DISCOMFORT ( 3 FDA reports)
ABDOMINAL DISTENSION ( 3 FDA reports)
ABNORMAL DREAMS ( 3 FDA reports)
ACUTE MYOCARDIAL INFARCTION ( 3 FDA reports)
AMNESIA ( 3 FDA reports)
ANURIA ( 3 FDA reports)
BLOOD CREATININE INCREASED ( 3 FDA reports)
BLOOD GLUCOSE DECREASED ( 3 FDA reports)
BLOOD PRESSURE DECREASED ( 3 FDA reports)
BLOOD UREA INCREASED ( 3 FDA reports)
BRADYCARDIA ( 3 FDA reports)
BRONCHOSPASM ( 3 FDA reports)
BURNING SENSATION ( 3 FDA reports)
CARDIAC ARREST ( 3 FDA reports)
CARDIAC MURMUR ( 3 FDA reports)
CEREBRAL HAEMATOMA ( 3 FDA reports)
CHOLESTASIS ( 3 FDA reports)
DEATH ( 3 FDA reports)
DISSOCIATION ( 3 FDA reports)
DISTURBANCE IN ATTENTION ( 3 FDA reports)
DRUG DEPENDENCE ( 3 FDA reports)
DRUG HYPERSENSITIVITY ( 3 FDA reports)
DYSARTHRIA ( 3 FDA reports)
DYSPNOEA EXERTIONAL ( 3 FDA reports)
DYSURIA ( 3 FDA reports)
ELECTROCARDIOGRAM POOR R-WAVE PROGRESSION ( 3 FDA reports)
ERYTHEMA ( 3 FDA reports)
ESCHAR ( 3 FDA reports)
EXTRASYSTOLES ( 3 FDA reports)
EYE PAIN ( 3 FDA reports)
FEELING HOT ( 3 FDA reports)
FEMUR FRACTURE ( 3 FDA reports)
FIBROSIS ( 3 FDA reports)
FLUID RETENTION ( 3 FDA reports)
GASTROINTESTINAL HAEMORRHAGE ( 3 FDA reports)
HALLUCINATION, VISUAL ( 3 FDA reports)
HEART RATE INCREASED ( 3 FDA reports)
HEPATIC ENZYME INCREASED ( 3 FDA reports)
HEPATITIS CHOLESTATIC ( 3 FDA reports)
HIGH DENSITY LIPOPROTEIN DECREASED ( 3 FDA reports)
HIP FRACTURE ( 3 FDA reports)
HYDROCEPHALUS ( 3 FDA reports)
JOINT CONTRACTURE ( 3 FDA reports)
JOINT STIFFNESS ( 3 FDA reports)
LIVER FUNCTION TEST ABNORMAL ( 3 FDA reports)
MENTAL IMPAIRMENT ( 3 FDA reports)
MOOD ALTERED ( 3 FDA reports)
MOUTH ULCERATION ( 3 FDA reports)
MUSCLE TIGHTNESS ( 3 FDA reports)
MUSCULOSKELETAL STIFFNESS ( 3 FDA reports)
NOCTURIA ( 3 FDA reports)
OBSESSIVE-COMPULSIVE DISORDER ( 3 FDA reports)
OEDEMA ( 3 FDA reports)
PERICARDIAL EFFUSION ( 3 FDA reports)
PHARYNGEAL OEDEMA ( 3 FDA reports)
PNEUMONITIS CHEMICAL ( 3 FDA reports)
PRESYNCOPE ( 3 FDA reports)
RENAL INJURY ( 3 FDA reports)
RESPIRATORY DISTRESS ( 3 FDA reports)
RESPIRATORY TRACT INFECTION FUNGAL ( 3 FDA reports)
SCAR ( 3 FDA reports)
SHOULDER PAIN ( 3 FDA reports)
SIGMOIDECTOMY ( 3 FDA reports)
SILENT MYOCARDIAL INFARCTION ( 3 FDA reports)
SINUS CONGESTION ( 3 FDA reports)
SINUS DISORDER ( 3 FDA reports)
SKIN HYPERTROPHY ( 3 FDA reports)
SKIN INDURATION ( 3 FDA reports)
SKIN PLAQUE ( 3 FDA reports)
SKIN TIGHTNESS ( 3 FDA reports)
SLEEP APNOEA SYNDROME ( 3 FDA reports)
SOCIAL AVOIDANT BEHAVIOUR ( 3 FDA reports)
THERAPEUTIC RESPONSE DECREASED ( 3 FDA reports)
THERAPEUTIC RESPONSE INCREASED ( 3 FDA reports)
THERAPY NON-RESPONDER ( 3 FDA reports)
UNEVALUABLE EVENT ( 3 FDA reports)
VERTIGO ( 3 FDA reports)
ADVERSE DRUG REACTION ( 2 FDA reports)
AGGRESSION ( 2 FDA reports)
ANAPHYLACTIC REACTION ( 2 FDA reports)
ANGIONEUROTIC OEDEMA ( 2 FDA reports)
ANOREXIA ( 2 FDA reports)
ASTHMA ( 2 FDA reports)
AZYGOS LOBE ( 2 FDA reports)
BACK DISORDER ( 2 FDA reports)
BILIARY DYSKINESIA ( 2 FDA reports)
BLADDER CANCER ( 2 FDA reports)
BLOOD CREATINE PHOSPHOKINASE INCREASED ( 2 FDA reports)
BLOOD POTASSIUM DECREASED ( 2 FDA reports)
BLOOD PRESSURE SYSTOLIC INCREASED ( 2 FDA reports)
BODY TEMPERATURE INCREASED ( 2 FDA reports)
BRADYPHRENIA ( 2 FDA reports)
CARDIOMEGALY ( 2 FDA reports)
COAGULOPATHY ( 2 FDA reports)
COLON CANCER ( 2 FDA reports)
COMA ( 2 FDA reports)
CONTUSION ( 2 FDA reports)
CONVULSION ( 2 FDA reports)
CYANOSIS ( 2 FDA reports)
CYSTITIS ( 2 FDA reports)
CYTOLYTIC HEPATITIS ( 2 FDA reports)
DECREASED ACTIVITY ( 2 FDA reports)
DEPRESSED LEVEL OF CONSCIOUSNESS ( 2 FDA reports)
DIABETES MELLITUS NON-INSULIN-DEPENDENT ( 2 FDA reports)
DIARRHOEA HAEMORRHAGIC ( 2 FDA reports)
DRUG DISPENSING ERROR ( 2 FDA reports)
DRUG EFFECT DECREASED ( 2 FDA reports)
DYSHIDROSIS ( 2 FDA reports)
EARLY SATIETY ( 2 FDA reports)
ECCHYMOSIS ( 2 FDA reports)
ECZEMA ( 2 FDA reports)
EJECTION FRACTION DECREASED ( 2 FDA reports)
EMOTIONAL DISORDER ( 2 FDA reports)
ERECTILE DYSFUNCTION ( 2 FDA reports)
EYE DISORDER ( 2 FDA reports)
EYE IRRITATION ( 2 FDA reports)
EYE SWELLING ( 2 FDA reports)
FEELING COLD ( 2 FDA reports)
FEELING JITTERY ( 2 FDA reports)
FLUID OVERLOAD ( 2 FDA reports)
FUNGAL SKIN INFECTION ( 2 FDA reports)
GALLBLADDER CHOLESTEROLOSIS ( 2 FDA reports)
GALLBLADDER DISORDER ( 2 FDA reports)
GASTRIC ULCER ( 2 FDA reports)
HAEMATEMESIS ( 2 FDA reports)
HAEMATOCRIT DECREASED ( 2 FDA reports)
HAEMODIALYSIS ( 2 FDA reports)
HAEMORRHAGE ( 2 FDA reports)
HANGOVER ( 2 FDA reports)
HELICOBACTER INFECTION ( 2 FDA reports)
HEMIPARESIS ( 2 FDA reports)
HEPATITIS ( 2 FDA reports)
HICCUPS ( 2 FDA reports)
HUNGER ( 2 FDA reports)
HYPERLIPIDAEMIA ( 2 FDA reports)
HYPERTONIC BLADDER ( 2 FDA reports)
HYPOALBUMINAEMIA ( 2 FDA reports)
IDIOPATHIC THROMBOCYTOPENIC PURPURA ( 2 FDA reports)
INCORRECT DOSE ADMINISTERED ( 2 FDA reports)
INCORRECT DRUG ADMINISTRATION DURATION ( 2 FDA reports)
INJECTION SITE HAEMATOMA ( 2 FDA reports)
INTERSTITIAL LUNG DISEASE ( 2 FDA reports)
IRRITABILITY ( 2 FDA reports)
JAUNDICE ( 2 FDA reports)
LARYNGOSPASM ( 2 FDA reports)
LEFT VENTRICULAR DYSFUNCTION ( 2 FDA reports)
LETHARGY ( 2 FDA reports)
LOWER RESPIRATORY TRACT INFECTION ( 2 FDA reports)
LYMPHADENOPATHY ( 2 FDA reports)
MALNUTRITION ( 2 FDA reports)
MEDICATION ERROR ( 2 FDA reports)
METABOLIC ACIDOSIS ( 2 FDA reports)
METASTASIS ( 2 FDA reports)
MICTURITION URGENCY ( 2 FDA reports)
MOOD SWINGS ( 2 FDA reports)
MULTI-ORGAN DISORDER ( 2 FDA reports)
MUSCULOSKELETAL CHEST PAIN ( 2 FDA reports)
MUSCULOSKELETAL DISORDER ( 2 FDA reports)
NEPHROLITHIASIS ( 2 FDA reports)
NEUROPATHY PERIPHERAL ( 2 FDA reports)
NO THERAPEUTIC RESPONSE ( 2 FDA reports)
NON-CARDIAC CHEST PAIN ( 2 FDA reports)
OESOPHAGEAL ULCER ( 2 FDA reports)
OESOPHAGITIS ( 2 FDA reports)
OROPHARYNGEAL PAIN ( 2 FDA reports)
PANCREATIC CALCIFICATION ( 2 FDA reports)
PANCREATITIS CHRONIC ( 2 FDA reports)
PANIC ATTACK ( 2 FDA reports)
PERSONALITY CHANGE ( 2 FDA reports)
PERSONALITY DISORDER ( 2 FDA reports)
PERTUSSIS ( 2 FDA reports)
PNEUMONIA VIRAL ( 2 FDA reports)
PRODUCT SUBSTITUTION ISSUE ( 2 FDA reports)
PSYCHOTIC DISORDER ( 2 FDA reports)
PULMONARY OEDEMA ( 2 FDA reports)
RADICULOPATHY ( 2 FDA reports)
RASH ERYTHEMATOUS ( 2 FDA reports)
RASH PAPULAR ( 2 FDA reports)
RASH VESICULAR ( 2 FDA reports)
RESTLESSNESS ( 2 FDA reports)
RHINORRHOEA ( 2 FDA reports)
ROAD TRAFFIC ACCIDENT ( 2 FDA reports)
SALIVARY HYPERSECRETION ( 2 FDA reports)
SCAB ( 2 FDA reports)
SENSATION OF FOREIGN BODY ( 2 FDA reports)
SENSORY LOSS ( 2 FDA reports)
SEXUAL DYSFUNCTION ( 2 FDA reports)
SPEECH DISORDER ( 2 FDA reports)
SPINAL DECOMPRESSION ( 2 FDA reports)
SPINAL DEFORMITY ( 2 FDA reports)
STOMACH DISCOMFORT ( 2 FDA reports)
SUICIDAL IDEATION ( 2 FDA reports)
SWOLLEN TONGUE ( 2 FDA reports)
TACHYARRHYTHMIA ( 2 FDA reports)
TARDIVE DYSKINESIA ( 2 FDA reports)
TEMPERATURE INTOLERANCE ( 2 FDA reports)
THINKING ABNORMAL ( 2 FDA reports)
THOUGHT INSERTION ( 2 FDA reports)
THROMBOSIS ( 2 FDA reports)
TOXIC SKIN ERUPTION ( 2 FDA reports)
TOXICITY TO VARIOUS AGENTS ( 2 FDA reports)
TRACHEOBRONCHITIS ( 2 FDA reports)
TREATMENT NONCOMPLIANCE ( 2 FDA reports)
TYPE 2 DIABETES MELLITUS ( 2 FDA reports)
ULCER ( 2 FDA reports)
URINARY TRACT INFECTION BACTERIAL ( 2 FDA reports)
UROSEPSIS ( 2 FDA reports)
VENOUS PRESSURE JUGULAR INCREASED ( 2 FDA reports)
VENTRICULAR TACHYCARDIA ( 2 FDA reports)
VISUAL ACUITY REDUCED ( 2 FDA reports)
ABASIA ( 1 FDA reports)
ABNORMAL FAECES ( 1 FDA reports)
ABNORMAL SENSATION IN EYE ( 1 FDA reports)
ABSCESS SOFT TISSUE ( 1 FDA reports)
ACTIVITIES OF DAILY LIVING IMPAIRED ( 1 FDA reports)
ACUTE PULMONARY OEDEMA ( 1 FDA reports)
ACUTE RESPIRATORY FAILURE ( 1 FDA reports)
ACUTE SINUSITIS ( 1 FDA reports)
ADENOCARCINOMA PANCREAS ( 1 FDA reports)
ADRENAL NEOPLASM ( 1 FDA reports)
AGITATION ( 1 FDA reports)
AKINESIA ( 1 FDA reports)
ALDOSTERONE URINE DECREASED ( 1 FDA reports)
ALVEOLOPLASTY ( 1 FDA reports)
ANAL DISCOMFORT ( 1 FDA reports)
ANAL PRURITUS ( 1 FDA reports)
ANAPHYLACTIC SHOCK ( 1 FDA reports)
ANEURYSM ( 1 FDA reports)
ANOMALY OF EXTERNAL EAR CONGENITAL ( 1 FDA reports)
ANTIPSYCHOTIC DRUG LEVEL INCREASED ( 1 FDA reports)
AORTIC STENOSIS ( 1 FDA reports)
AORTIC VALVE INCOMPETENCE ( 1 FDA reports)
APHASIA ( 1 FDA reports)
APPLICATION SITE HAEMATOMA ( 1 FDA reports)
ARRHYTHMIA ( 1 FDA reports)
ARTERIAL DISORDER ( 1 FDA reports)
ARTERIAL THROMBOSIS ( 1 FDA reports)
ARTERIOGRAM CORONARY ( 1 FDA reports)
ARTHROPATHY ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK ( 1 FDA reports)
ATRIOVENTRICULAR BLOCK COMPLETE ( 1 FDA reports)
AXILLARY MASS ( 1 FDA reports)
BALANCE DISORDER ( 1 FDA reports)
BILE DUCT CANCER ( 1 FDA reports)
BLADDER DISORDER ( 1 FDA reports)
BLADDER TRANSITIONAL CELL CARCINOMA STAGE II ( 1 FDA reports)
BLINDNESS ( 1 FDA reports)
BLINDNESS TRANSIENT ( 1 FDA reports)
BLINDNESS UNILATERAL ( 1 FDA reports)
BLOOD BICARBONATE ( 1 FDA reports)
BLOOD CREATININE ( 1 FDA reports)
BLOOD MAGNESIUM ( 1 FDA reports)
BLOOD PRESSURE NORMAL ( 1 FDA reports)
BLOOD SODIUM DECREASED ( 1 FDA reports)
BLOOD TESTOSTERONE DECREASED ( 1 FDA reports)
BLOOD THYROID STIMULATING HORMONE DECREASED ( 1 FDA reports)
BLOOD UREA ( 1 FDA reports)
BLOOD URIC ACID ( 1 FDA reports)
BLOOD URIC ACID INCREASED ( 1 FDA reports)
BONE MARROW FAILURE ( 1 FDA reports)
BREAST CANCER ( 1 FDA reports)
BRONCHIAL DISORDER ( 1 FDA reports)
BUNDLE BRANCH BLOCK LEFT ( 1 FDA reports)
BUNDLE BRANCH BLOCK RIGHT ( 1 FDA reports)
CARDIOGENIC SHOCK ( 1 FDA reports)
CARDIOLIPIN ANTIBODY POSITIVE ( 1 FDA reports)
CARDIOMYOPATHY ( 1 FDA reports)
CAROTID ARTERY STENOSIS ( 1 FDA reports)
CATARACT ( 1 FDA reports)
CAUSTIC INJURY ( 1 FDA reports)
CENTRAL NERVOUS SYSTEM LYMPHOMA ( 1 FDA reports)
CEREBELLAR INFARCTION ( 1 FDA reports)
CEREBRAL ARTERY OCCLUSION ( 1 FDA reports)
CEREBRAL ARTERY THROMBOSIS ( 1 FDA reports)
CEREBRAL INFARCTION ( 1 FDA reports)
CEREBRAL ISCHAEMIA ( 1 FDA reports)
CEREBRAL VENTRICLE DILATATION ( 1 FDA reports)
CHEST X-RAY ( 1 FDA reports)
CHEST X-RAY ABNORMAL ( 1 FDA reports)
CHOKING ( 1 FDA reports)
CHOLECYSTECTOMY ( 1 FDA reports)
CHRONIC FATIGUE SYNDROME ( 1 FDA reports)
CHRONIC LYMPHOCYTIC LEUKAEMIA ( 1 FDA reports)
CIRCADIAN RHYTHM SLEEP DISORDER ( 1 FDA reports)
COGNITIVE DISORDER ( 1 FDA reports)
COGWHEEL RIGIDITY ( 1 FDA reports)
COLLAPSE OF LUNG ( 1 FDA reports)
CONJUNCTIVAL HYPERAEMIA ( 1 FDA reports)
CORONARY ARTERY OCCLUSION ( 1 FDA reports)
CORONARY ARTERY STENOSIS ( 1 FDA reports)
CRYING ( 1 FDA reports)
CYSTITIS ESCHERICHIA ( 1 FDA reports)
CYTOGENETIC ABNORMALITY ( 1 FDA reports)
DEEP VEIN THROMBOSIS ( 1 FDA reports)
DELIRIUM ( 1 FDA reports)
DELIRIUM TREMENS ( 1 FDA reports)
DELUSION ( 1 FDA reports)
DELUSION OF REFERENCE ( 1 FDA reports)
DEMENTIA ( 1 FDA reports)
DEMYELINATION ( 1 FDA reports)
DEPRESSIVE SYMPTOM ( 1 FDA reports)
DERMATITIS BULLOUS ( 1 FDA reports)
DEVICE INTERACTION ( 1 FDA reports)
DIABETES INSIPIDUS ( 1 FDA reports)
DIABETIC KETOACIDOSIS ( 1 FDA reports)
DIABETIC NEUROPATHY ( 1 FDA reports)
DIALYSIS ( 1 FDA reports)
DIPLOPIA ( 1 FDA reports)
DISEASE RECURRENCE ( 1 FDA reports)
DISORIENTATION ( 1 FDA reports)
DIZZINESS POSTURAL ( 1 FDA reports)
DRUG ADMINISTRATION ERROR ( 1 FDA reports)
DRUG ERUPTION ( 1 FDA reports)
DRUG SCREEN POSITIVE ( 1 FDA reports)
DRY EYE ( 1 FDA reports)
DRY SKIN ( 1 FDA reports)
DRY THROAT ( 1 FDA reports)
DUODENITIS ( 1 FDA reports)
DYSAESTHESIA ( 1 FDA reports)
DYSFUNCTIONAL UTERINE BLEEDING ( 1 FDA reports)
DYSMENORRHOEA ( 1 FDA reports)
DYSPHONIA ( 1 FDA reports)
DYSTHYMIC DISORDER ( 1 FDA reports)
ECONOMIC PROBLEM ( 1 FDA reports)
ECZEMA VESICULAR ( 1 FDA reports)
ELECTROCARDIOGRAM ( 1 FDA reports)
ELECTROCARDIOGRAM ABNORMAL ( 1 FDA reports)
ELECTROCARDIOGRAM QT PROLONGED ( 1 FDA reports)
ELECTROLYTE IMBALANCE ( 1 FDA reports)
ERECTION INCREASED ( 1 FDA reports)
ESSENTIAL TREMOR ( 1 FDA reports)
EUPHORIC MOOD ( 1 FDA reports)
EXCESSIVE GRANULATION TISSUE ( 1 FDA reports)
EXERCISE TOLERANCE DECREASED ( 1 FDA reports)
EXPIRED DRUG ADMINISTERED ( 1 FDA reports)
EXTRAPYRAMIDAL DISORDER ( 1 FDA reports)
FACIAL PAIN ( 1 FDA reports)
FACIAL PALSY ( 1 FDA reports)
FAECES DISCOLOURED ( 1 FDA reports)
FEBRILE NEUTROPENIA ( 1 FDA reports)
FIBROMYALGIA ( 1 FDA reports)
FRACTURE ( 1 FDA reports)
FRUSTRATION ( 1 FDA reports)
GANGRENE ( 1 FDA reports)
GASTRIC NEOPLASM ( 1 FDA reports)
GASTRIC ULCER HAEMORRHAGE ( 1 FDA reports)
GASTROENTERITIS ( 1 FDA reports)
GASTROINTESTINAL DISORDER ( 1 FDA reports)
GASTROINTESTINAL PAIN ( 1 FDA reports)
GINGIVITIS ( 1 FDA reports)
GLAUCOMA ( 1 FDA reports)
GLOMERULAR FILTRATION RATE ( 1 FDA reports)
GOUTY ARTHRITIS ( 1 FDA reports)
HAEMATOCHEZIA ( 1 FDA reports)
HAEMORRHAGIC STROKE ( 1 FDA reports)
HEAD INJURY ( 1 FDA reports)
HEARING IMPAIRED ( 1 FDA reports)
HEPATIC FIBROSIS ( 1 FDA reports)
HEPATIC NECROSIS ( 1 FDA reports)
HEPATIC STEATOSIS ( 1 FDA reports)
HEPATITIS FULMINANT ( 1 FDA reports)
HERPES ZOSTER DISSEMINATED ( 1 FDA reports)
HIATUS HERNIA ( 1 FDA reports)
HIGH DENSITY LIPOPROTEIN INCREASED ( 1 FDA reports)
HOSPITALISATION ( 1 FDA reports)
HYPERCALCAEMIA ( 1 FDA reports)
HYPERCHOLESTEROLAEMIA ( 1 FDA reports)
HYPERKINESIA ( 1 FDA reports)
HYPERPHAGIA ( 1 FDA reports)
HYPERPHOSPHATAEMIA ( 1 FDA reports)
HYPERTENSIVE CRISIS ( 1 FDA reports)
HYPERTENSIVE ENCEPHALOPATHY ( 1 FDA reports)
HYPERTENSIVE HEART DISEASE ( 1 FDA reports)
HYPERTHYROIDISM ( 1 FDA reports)
HYPERTRICHOSIS ( 1 FDA reports)
HYPERVITAMINOSIS ( 1 FDA reports)
HYPOCALCAEMIA ( 1 FDA reports)
HYPOMAGNESAEMIA ( 1 FDA reports)
HYPOPHYSITIS ( 1 FDA reports)
HYPOTHYROIDISM ( 1 FDA reports)
HYPOTONIA ( 1 FDA reports)
HYPOVOLAEMIC SHOCK ( 1 FDA reports)
ILIAC ARTERY STENOSIS ( 1 FDA reports)
ILL-DEFINED DISORDER ( 1 FDA reports)
IMMUNOSUPPRESSANT DRUG LEVEL INCREASED ( 1 FDA reports)
IMPAIRED GASTRIC EMPTYING ( 1 FDA reports)
IMPAIRED WORK ABILITY ( 1 FDA reports)
INAPPROPRIATE ANTIDIURETIC HORMONE SECRETION ( 1 FDA reports)
INCISION SITE INFECTION ( 1 FDA reports)
INCOHERENT ( 1 FDA reports)
INCONTINENCE ( 1 FDA reports)
INCREASED APPETITE ( 1 FDA reports)
INFECTED SKIN ULCER ( 1 FDA reports)
INFECTION ( 1 FDA reports)
INFLUENZA LIKE ILLNESS ( 1 FDA reports)
INFUSION RELATED REACTION ( 1 FDA reports)
INGUINAL HERNIA, OBSTRUCTIVE ( 1 FDA reports)
INJECTION SITE HAEMORRHAGE ( 1 FDA reports)
INJECTION SITE INJURY ( 1 FDA reports)
INTENTIONAL OVERDOSE ( 1 FDA reports)
INTERNATIONAL NORMALISED RATIO DECREASED ( 1 FDA reports)
INTESTINAL OBSTRUCTION ( 1 FDA reports)
INTRAVENTRICULAR HAEMORRHAGE ( 1 FDA reports)
ISCHAEMIC STROKE ( 1 FDA reports)
JAUNDICE CHOLESTATIC ( 1 FDA reports)
JOINT INJURY ( 1 FDA reports)
JOINT SWELLING ( 1 FDA reports)
KIDNEY TRANSPLANT REJECTION ( 1 FDA reports)
LABORATORY TEST ( 1 FDA reports)
LARGE INTESTINE PERFORATION ( 1 FDA reports)
LEFT VENTRICULAR FAILURE ( 1 FDA reports)
LEFT VENTRICULAR HYPERTROPHY ( 1 FDA reports)
LEUKOCYTOCLASTIC VASCULITIS ( 1 FDA reports)
LEUKOPENIA ( 1 FDA reports)
LIGAMENT RUPTURE ( 1 FDA reports)
LIMB DISCOMFORT ( 1 FDA reports)
LIMB INJURY ( 1 FDA reports)
LIMB OPERATION ( 1 FDA reports)
LIP OEDEMA ( 1 FDA reports)
LIP SWELLING ( 1 FDA reports)
LIP ULCERATION ( 1 FDA reports)
LIPOMA ( 1 FDA reports)
LIPOSARCOMA ( 1 FDA reports)
LIVER DISORDER ( 1 FDA reports)
LIVER TRANSPLANT ( 1 FDA reports)
LUNG NEOPLASM ( 1 FDA reports)
LUNG NEOPLASM MALIGNANT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA RECURRENT ( 1 FDA reports)
LUNG SQUAMOUS CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
LYMPHOCELE ( 1 FDA reports)
MACULOPATHY ( 1 FDA reports)
MANIA ( 1 FDA reports)
MARKEDLY REDUCED DIETARY INTAKE ( 1 FDA reports)
MASS ( 1 FDA reports)
MATERNAL DRUGS AFFECTING FOETUS ( 1 FDA reports)
MATERNAL EXPOSURE DURING PREGNANCY ( 1 FDA reports)
MEDICAL DEVICE COMPLICATION ( 1 FDA reports)
MEMORY IMPAIRMENT ( 1 FDA reports)
MENINGIOMA ( 1 FDA reports)
MENTAL DISORDER ( 1 FDA reports)
MESANGIOPROLIFERATIVE GLOMERULONEPHRITIS ( 1 FDA reports)
METASTASES TO LIVER ( 1 FDA reports)
MICROANGIOPATHY ( 1 FDA reports)
MIGRAINE ( 1 FDA reports)
MITRAL VALVE INCOMPETENCE ( 1 FDA reports)
MOVEMENT DISORDER ( 1 FDA reports)
MUSCLE DISORDER ( 1 FDA reports)
MUSCLE FATIGUE ( 1 FDA reports)
MUSCLE TWITCHING ( 1 FDA reports)
MYDRIASIS ( 1 FDA reports)
MYOGLOBIN BLOOD INCREASED ( 1 FDA reports)
MYOPATHY ( 1 FDA reports)
MYOPERICARDITIS ( 1 FDA reports)
NAIL DISORDER ( 1 FDA reports)
NASAL CONGESTION ( 1 FDA reports)
NASOPHARYNGITIS ( 1 FDA reports)
NEPHROANGIOSCLEROSIS ( 1 FDA reports)
NERVOUS SYSTEM DISORDER ( 1 FDA reports)
NEURALGIA ( 1 FDA reports)
NEUROENDOCRINE TUMOUR ( 1 FDA reports)
NEUROPATHY ( 1 FDA reports)
OCULAR HYPERAEMIA ( 1 FDA reports)
OCULAR VASCULAR DISORDER ( 1 FDA reports)
OEDEMA MOUTH ( 1 FDA reports)
OESOPHAGEAL DISCOMFORT ( 1 FDA reports)
ORAL ADMINISTRATION COMPLICATION ( 1 FDA reports)
ORAL FUNGAL INFECTION ( 1 FDA reports)
ORAL HERPES ( 1 FDA reports)
ORAL INFECTION ( 1 FDA reports)
ORAL NEOPLASM ( 1 FDA reports)
ORAL PAIN ( 1 FDA reports)
ORGANISING PNEUMONIA ( 1 FDA reports)
ORTHOSTATIC HYPOTENSION ( 1 FDA reports)
OTITIS MEDIA ( 1 FDA reports)
PAINFUL ERECTION ( 1 FDA reports)
PANCREATIC CARCINOMA ( 1 FDA reports)
PANCREATIC MASS ( 1 FDA reports)
PANCREATIC PSEUDOCYST ( 1 FDA reports)
PARASOMNIA ( 1 FDA reports)
PARITY ( 1 FDA reports)
PEMPHIGOID ( 1 FDA reports)
PEPTIC ULCER REACTIVATED ( 1 FDA reports)
PERIORBITAL OEDEMA ( 1 FDA reports)
PERIPHERAL ISCHAEMIA ( 1 FDA reports)
PERIPHERAL VASCULAR DISORDER ( 1 FDA reports)
PERITONITIS ( 1 FDA reports)
PERITONITIS BACTERIAL ( 1 FDA reports)
PETECHIAE ( 1 FDA reports)
PHYSICAL DISABILITY ( 1 FDA reports)
PLEURISY ( 1 FDA reports)
PNEUMONIA ASPIRATION ( 1 FDA reports)
POLYOMAVIRUS TEST POSITIVE ( 1 FDA reports)
POST PROCEDURAL COMPLICATION ( 1 FDA reports)
POST-TRAUMATIC STRESS DISORDER ( 1 FDA reports)
PRESSURE OF SPEECH ( 1 FDA reports)
PROCEDURAL COMPLICATION ( 1 FDA reports)
PRODUCT COLOUR ISSUE ( 1 FDA reports)
PRODUCTIVE COUGH ( 1 FDA reports)
PROSTATIC SPECIFIC ANTIGEN INCREASED ( 1 FDA reports)
PSORIASIS ( 1 FDA reports)
PSYCHOMOTOR HYPERACTIVITY ( 1 FDA reports)
PULMONARY EMBOLISM ( 1 FDA reports)
PURULENCE ( 1 FDA reports)
QUALITY OF LIFE DECREASED ( 1 FDA reports)
RASH MACULAR ( 1 FDA reports)
RASH MACULO-PAPULAR ( 1 FDA reports)
RASH PRURITIC ( 1 FDA reports)
RED BLOOD CELL COUNT ( 1 FDA reports)
RENAL CELL CARCINOMA STAGE UNSPECIFIED ( 1 FDA reports)
RENAL FAILURE CHRONIC ( 1 FDA reports)
RENAL FUNCTION TEST ABNORMAL ( 1 FDA reports)
RENAL NEOPLASM ( 1 FDA reports)
RESPIRATORY DISORDER ( 1 FDA reports)
RESPIRATORY RATE INCREASED ( 1 FDA reports)
RHEUMATOID ARTHRITIS ( 1 FDA reports)
ROSACEA ( 1 FDA reports)
RUPTURED CEREBRAL ANEURYSM ( 1 FDA reports)
SCOLIOSIS ( 1 FDA reports)
SCREAMING ( 1 FDA reports)
SECRETION DISCHARGE ( 1 FDA reports)
SEMEN DISCOLOURATION ( 1 FDA reports)
SEMEN VOLUME DECREASED ( 1 FDA reports)
SENSE OF OPPRESSION ( 1 FDA reports)
SENSORY DISTURBANCE ( 1 FDA reports)
SHOCK ( 1 FDA reports)
SHOCK HYPOGLYCAEMIC ( 1 FDA reports)
SINOATRIAL BLOCK ( 1 FDA reports)
SINUS ARREST ( 1 FDA reports)
SINUSITIS ( 1 FDA reports)
SKIN INFECTION ( 1 FDA reports)
SKIN IRRITATION ( 1 FDA reports)
SLEEP DISORDER DUE TO GENERAL MEDICAL CONDITION, INSOMNIA TYPE ( 1 FDA reports)
SNORING ( 1 FDA reports)
SPINAL LAMINECTOMY ( 1 FDA reports)
SQUAMOUS CELL CARCINOMA ( 1 FDA reports)
STENT PLACEMENT ( 1 FDA reports)
SUPRAVENTRICULAR TACHYCARDIA ( 1 FDA reports)
SYSTEMIC LUPUS ERYTHEMATOSUS ( 1 FDA reports)
TENDON PAIN ( 1 FDA reports)
THIRST ( 1 FDA reports)
THROAT IRRITATION ( 1 FDA reports)
THROAT TIGHTNESS ( 1 FDA reports)
THROMBOCYTOPENIA ( 1 FDA reports)
THROMBOEMBOLIC STROKE ( 1 FDA reports)
THROMBOSIS IN DEVICE ( 1 FDA reports)
THYROID DISORDER ( 1 FDA reports)
THYROID FUNCTION TEST ABNORMAL ( 1 FDA reports)
THYROID NEOPLASM ( 1 FDA reports)
TINNITUS ( 1 FDA reports)
TONGUE DISCOLOURATION ( 1 FDA reports)
TONGUE OEDEMA ( 1 FDA reports)
TONGUE ULCERATION ( 1 FDA reports)
TOOTH INJURY ( 1 FDA reports)
TRACHEITIS ( 1 FDA reports)
TRANSIENT GLOBAL AMNESIA ( 1 FDA reports)
TREATMENT FAILURE ( 1 FDA reports)
UPPER GASTROINTESTINAL HAEMORRHAGE ( 1 FDA reports)
UPPER RESPIRATORY TRACT INFECTION ( 1 FDA reports)
URINARY TRACT INFECTION ENTEROCOCCAL ( 1 FDA reports)
URINE ABNORMALITY ( 1 FDA reports)
URINE ANALYSIS ( 1 FDA reports)
URINE OUTPUT DECREASED ( 1 FDA reports)
VASCULAR PURPURA ( 1 FDA reports)
VASCULITIS ( 1 FDA reports)
VENTRICULAR HYPERTROPHY ( 1 FDA reports)
VIRAEMIA ( 1 FDA reports)
VIRAL INFECTION ( 1 FDA reports)
VISCERAL OEDEMA ( 1 FDA reports)
VITILIGO ( 1 FDA reports)
WHEEZING ( 1 FDA reports)
WHITE BLOOD CELL DISORDER ( 1 FDA reports)
WOUND DEBRIDEMENT ( 1 FDA reports)
WRONG DRUG ADMINISTERED ( 1 FDA reports)

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